Macadamia Diced Nuts packaged under the following brands: 1) Shurfine, Item no. 86635, 5 OZ (142 g) plastic bags, packed 12 bags per c...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (Salmonella contamination). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1244-2016.
Product potentially contaminated with Salmonella. Routine, random product sampling by FDA revealed the presence of Salmonella in a retail package of macadamia nuts packaged by the recalling firm.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1244-2016.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Marathon Ventures Inc or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1244-2016.
Marathon Ventures Inc
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Marathon Ventures Inc Recall FAQ
Marathon Ventures Inc is the subject of a food safety report: Macadamia Diced Nuts packaged under the following brands: 1) Shurfine, Item no. 86635, 5 OZ (142 g) plastic bags, packed 12 bags per c.... The notice was published on February 23, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 5,890 units are potentially affected.